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作 者:HOU Xuemei ZHAO Changjie TIAN Yanlong DOU Shuliang ZHANG Xiang ZHAO Jiupeng
机构地区:[1]School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin 150001, P. R. China [2]Center for Composite Materials, Harbin Institute of Technology, Harbin 150001, P. R. China
出 处:《Chemical Research in Chinese Universities》2016年第6期889-894,共6页高等学校化学研究(英文版)
摘 要:Magnetic Fe304@SiO2 nanoparticles with superparamagnetic properties were prepared via a reverse mi-croemulsion method at room temperature. The as-prepared samples were characterized by transmission electron mi-croscopy(TEM), X-ray diffractometry(XRD), and vibrating sample magnetometry(VSM). The Fe304@SiO2 nanopar-ticles were modified by (3-aminopropyl)triethoxysilane(APTES) and subsequently activated by glutaraldehyde(Glu).Protein A was successfully immobilized covalently onto the Glu activated Fe304@SiO2 nanoparticles. The adsorptioncapacity of the nanoparticles was determined on an ultraviolet spectrophotometer(UV) and approximately up to 203mg/g of protein A could be uniformly immobilized onto the modified Fe304@SiO2 magnetic beads. The core-shell ofthe Fe304@SiO2 magnetic beads decorated with protein A showed a good binding capacity for the chime-ric anti-EGFR monoclonal antibody(anti-EGFR mAb). The purity of the anti-EGFR mAb was analyzed by virtue ofHPLC. The protein A immobilized affinity beads provided a purity of about 95.4%.
关 键 词:Magnetic Fe304@SiO2 Protein A Nanoparticle MONOCLONAL ANTIBODY
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